Atara Biotherapeutics, Inc. (ATRA): History, Ownership, Mission, How It Works & Makes Money

Atara Biotherapeutics, Inc. (ATRA): History, Ownership, Mission, How It Works & Makes Money

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Atara Biotherapeutics, Inc. (ATRA) is pioneering allogeneic T-cell immunotherapy, but with a recent market capitalization of approximately $94.03 Million as of November 2025, how does a biotech with a laser-focus on one core asset navigate the high-risk drug development landscape? The strategic pivot to its partner, Pierre Fabre Laboratories, is key, as the company is now eligible for a crucial $40 Million milestone payment upon FDA approval of Tab-cel, which is a massive lever against a Q3 2025 net loss of just $4.3 Million. You need to know the mechanics behind this leaner model-which generated trailing twelve-month revenue of roughly $151.93 Million-to judge if this is a classic biotech turnaround or a defintely necessary restructuring to survive.

Atara Biotherapeutics, Inc. (ATRA) History

You need a clear picture of how Atara Biotherapeutics, Inc. (ATRA) got to its current, ultra-lean state. The story is one of a pivot from a broad cell therapy pipeline to a singular, high-stakes focus on its lead product, tabelecleucel (Ebvallo). The company was founded on the promise of off-the-shelf T-cell immunotherapies, but a series of costly clinical and regulatory hurdles forced a dramatic restructuring in 2025. This history of bold ambition followed by sharp strategic contraction is defintely the key to understanding its current valuation.

Given Company's Founding Timeline

Year established

The company was established in August 2012, aiming to pioneer allogeneic (off-the-shelf) T-cell therapies.

Original location

Operations began in South San Francisco, California, a hub for biotech innovation. Its current headquarters are in Thousand Oaks, California.

Founding team members

Key individuals involved in the founding included Isaac Ciechanover, MD, and Christopher Haqq, MD, PhD. The initial backing came from the founding venture investor, Kleiner Perkins Caufield & Byers (KPCB).

Initial capital/funding

Atara Biotherapeutics was launched with initial venture capital funding led by KPCB. The first major public capital injection came from its Initial Public Offering (IPO) in 2014, which raised approximately $85 million in gross proceeds to fuel its pipeline development.

Given Company's Evolution Milestones

Year Key Event Significance
2014 Initial Public Offering (IPO) on Nasdaq Raised approximately $85 million gross proceeds, providing the capital for rapid expansion of research and development.
2015 Acquired Cell Therapy Portfolio from Memorial Sloan Kettering Cancer Center (MSK) Gained rights to key T-cell therapy candidates, including the foundational technology for tabelecleucel (tab-cel), its lead product.
2017 Initiated Phase 3 studies for tab-cel Advanced its lead product into pivotal trials for Epstein-Barr virus positive post-transplant lymphoproliferative disease (EBV+ PTLD), moving closer to commercialization.
2025 (Jan) FDA issues Complete Response Letter (CRL) and clinical hold on tab-cel A major setback due to manufacturing inspection findings at a third-party site, forcing a complete strategic reassessment of the company's operational model.
2025 (Oct) Completed transfer of tab-cel activities and BLA sponsorship to Pierre Fabre The final step in the strategic pivot, dramatically cutting operational costs and reducing the workforce to only about 15 essential employees.
2025 (Nov) tab-cel BLA accepted for Priority Review by FDA Secured a PDUFA target action date of January 10, 2026, setting up a potential $40 million milestone payment from Pierre Fabre.

Given Company's Transformative Moments

The most transformative period for Atara Biotherapeutics was the dramatic strategic pivot in 2025, moving from a multi-asset developer to an ultra-lean entity focused purely on the success of its partnership with Pierre Fabre Laboratories. This was a survival move.

The financial impact is clear: in Q3 2025, total operating expenses plunged 89% year-over-year to just $7 million, with Research and Development (R&D) expenses dropping 93% to $2.9 million. This massive cost-cutting, driven by the transfer of the tab-cel program, narrowed the net loss to $4.3 million in Q3 2025, down from a $21.9 million loss in Q3 2024.

  • The CAR-T Discontinuation: In March 2025, the company announced the discontinuation of all CAR-T (Chimeric Antigen Receptor T-cell) operations, including ATA3219 and ATA3431. This decision marked the end of its internal allogeneic CAR-T ambitions to conserve capital.
  • The Pierre Fabre Deal Restructure: Following the FDA's CRL in January 2025, Atara Biotherapeutics transferred manufacturing, supply, and eventually the BLA sponsorship for tab-cel to Pierre Fabre. This offloaded nearly all associated costs and risk, but it also reduced the potential FDA approval milestone payment from an expected $60 million to $40 million.
  • Extreme Workforce Reduction: Multiple restructurings in 2025, including cuts in January, March, and October, reduced the company's size significantly. The final October 2025 restructuring retained only about 15 essential employees, reflecting a complete shift to a royalty and milestone-driven business model.

This history shows a company that aggressively streamlined to survive, essentially outsourcing its first commercial product to a partner to focus on financial longevity. You can see the full financial picture and what this means for the future in Breaking Down Atara Biotherapeutics, Inc. (ATRA) Financial Health: Key Insights for Investors.

Atara Biotherapeutics, Inc. (ATRA) Ownership Structure

The ownership of Atara Biotherapeutics, Inc. (ATRA) is highly concentrated, with a significant portion held by venture capital funds and insiders, which gives them substantial influence over the company's strategic direction and governance.

This structure means a few key stakeholders, rather than the broad public market, hold the majority of the voting power, a common scenario for a biotech company in a pivotal regulatory phase, like the one Atara is in with its tabelecleucel (tab-cel) program.

Given Company's Current Status

Atara Biotherapeutics is a publicly held, clinical-stage biopharmaceutical company. Its common stock is traded on the Nasdaq Stock Market LLC under the ticker symbol ATRA.

As of November 2025, the company has undergone a major operational shift, focusing on capital efficiency by transferring substantially all tab-cel activities, including the Biologics License Application (BLA) sponsorship, to its partner, Pierre Fabre Laboratories. This strategic pivot is projected to reduce 2025 operating expenses by at least 60% compared to 2024. That's a huge cost-saving move.

The company reported a net loss of $4.3 million for the third quarter of fiscal year 2025, a significant improvement from the $21.9 million loss in the same period in 2024.

Given Company's Ownership Breakdown

The company's ownership is dominated by a few large venture capital firms, which are classified as insiders due to their board representation and influence. This high insider ownership, which is around 42.40%, is the single most important factor in understanding who controls the company.

For example, Panacea Innovation Ltd is the largest single shareholder, owning approximately 38.95% of the company's shares. This level of concentration means management decisions are defintely tied to the interests of these major strategic investors. You can see the full financial picture, including the impact of these strategic shifts, at Breaking Down Atara Biotherapeutics, Inc. (ATRA) Financial Health: Key Insights for Investors.

Shareholder Type Ownership, % Notes
Insider Ownership (VC/Management) 42.40% Includes major venture capital funds like Panacea Innovation Ltd (approx. 38.95%) and Adiumentum Capital Fund I LP (approx. 17.22%), which exert significant control.
General Institutional Investors 25.93% Held by funds like Vanguard Group Inc, BlackRock, Inc., and EcoR1 Capital, LLC.
Retail and Public Float 31.67% The remaining shares held by individual investors and smaller public entities.

Given Company's Leadership

The leadership team has seen significant changes in 2025, reflecting the company's shift toward a leaner, more focused operational model. The average tenure for the current management team is quite short, suggesting a new era of governance focused on fiscal discipline.

  • President and CEO: Cokey Nguyen, Ph.D. He was appointed in September 2024 and is driving the strategic focus on the allogeneic T-cell platform.
  • Chairman of the Board: Gregory A. Ciongoli. He was elevated to this role in September 2025, signaling a board pivot toward prioritizing fiscal discipline.
  • Chief Accounting Officer: Yanina Grant-Huerta. She signed the latest SEC filings in November 2025.
  • EVP and Chief Legal Officer: K. Amar Murugan. He has been with the company since 2023.

The board restructuring in September 2025, which saw the departure of the former Chair and other directors, was explicitly done to align the board with the company's reduced size and streamlined operations. They are cutting costs and focusing on the BLA approval for tab-cel, which could unlock a $40 million milestone payment from Pierre Fabre Laboratories.

Atara Biotherapeutics, Inc. (ATRA) Mission and Values

Atara Biotherapeutics, Inc. exists to transform the lives of patients with serious diseases, moving beyond traditional small-molecule drugs to pioneer allogeneic T-cell immunotherapies (off-the-shelf cell treatments). This core purpose is grounded in a set of values that prioritize scientific excellence and patient impact over everything else, which is defintely a necessary focus given their current financial restructuring.

You're looking at a company that is fundamentally driven by its science, but you also need to see the financial reality: their Q3 2025 net loss was $4.3 million, a significant improvement from the prior year, but still a loss. The mission is what justifies the aggressive cost-cutting-like the projected 60%+ reduction in 2025 operating expenses-to extend the cash runway and deliver on the promise of the platform.

Given Company's Core Purpose

The company's mission and values provide the cultural DNA, telling you where their capital and human resources are truly focused. For a biotech firm like Atara Biotherapeutics, this non-financial framework is a critical indicator of long-term resilience and strategic focus, especially as they pivot to a more streamlined, royalty-focused model following the tabelecleucel (tab-cel) partnership with Pierre Fabre Laboratories.

Official Mission Statement

The mission is a clear, one-line directive that guides every research and development dollar spent. It's simple: transform patient lives through innovative cell therapies. Honestly, this mission is the engine that drives their risk-taking in the challenging field of allogeneic T-cell immunotherapy (donor-derived cell therapy).

  • Transform the lives of patients with serious diseases.
  • Achieve this through pioneering science and a commitment to excellence.
  • Focus on leveraging the allogeneic T-cell platform to address significant unmet medical needs.

Vision Statement

Atara Biotherapeutics' vision is about being a pioneer and a global leader in a very specific, high-potential area of medicine. They aren't just looking for one product; they want to build a platform that can treat a wide range of diseases, from cancer to autoimmune conditions.

  • Be at the forefront of cell therapy advancements, continuously refining their allogeneic T-cell platform.
  • Address unmet medical needs by creating therapies for diseases with limited or no effective treatment options.
  • Expand therapeutic applications to treat various cancers, autoimmune conditions, and viral infections.

Their focus is on delivering off-the-shelf treatments, which is the holy grail of cell therapy because it means rapid delivery from inventory, not a long wait for a patient's own cells to be engineered. This is a huge competitive edge.

Given Company Slogan/Tagline

The most powerful phrase they use cuts straight to their scientific ambition.

  • UNLEASHING THE PROMISE OF T-CELL THERAPIES.

This tagline perfectly captures their belief in the immune system's natural power. It's a bold statement, but they have the first-ever regulatory approval for an allogeneic T-cell immunotherapy (EBVALLO in Europe) to back it up. This is the kind of clinical validation that makes the potential $40 million FDA approval milestone payment for tab-cel so critical to their near-term financial future.

You can dig deeper into how these principles guide their decisions here: Mission Statement, Vision, & Core Values of Atara Biotherapeutics, Inc. (ATRA).

The company formalizes its ethical framework through the TRAIT values, which stand for Transparency, Respect, Accountability, Integrity, and Trust. This is their internal compass for everything, from clinical trial reporting to the October 2025 organizational restructuring that impacted approximately 29% of employees.

Atara Biotherapeutics, Inc. (ATRA) How It Works

Atara Biotherapeutics, Inc. operates by leveraging the natural power of the immune system to create off-the-shelf (allogeneic) T-cell immunotherapies, which are cell therapies derived from a healthy third-party donor instead of the patient's own cells.

This approach allows for rapid delivery to patients from inventory, sidestepping the complex, time-consuming logistics of personalized (autologous) cell therapies, and focuses on treating difficult-to-treat cancers and autoimmune conditions, particularly those driven by the Epstein-Barr virus (EBV).

Atara Biotherapeutics, Inc.'s Product/Service Portfolio

Following a significant strategic shift in 2025 to focus on the value of its lead asset, the portfolio is now streamlined. The company has substantially transitioned its commercialization and regulatory activities for its lead product to its partner, Pierre Fabre Laboratories.

Product/Service Target Market Key Features
Tabelecleucel (tab-cel®) / Ebvallo™ Epstein-Barr Virus positive Post-Transplant Lymphoproliferative Disease (EBV+ PTLD) First-in-class, off-the-shelf allogeneic T-cell immunotherapy; FDA BLA resubmission accepted with a PDUFA date of January 10, 2026; already approved in the European Economic Area.
ATA188 Progressive Multiple Sclerosis (PMS) Investigational T-cell therapy targeting EBV-infected B cells and plasma cells, which are believed to be a root cause of MS; in clinical development.
ATA227 Autoimmune Indications Earlier-stage investigational T-cell therapy targeting various B-cell driven autoimmune disorders.

Atara Biotherapeutics, Inc.'s Operational Framework

The company's operational framework underwent a dramatic shift in 2025, moving from a full-scale biopharma model to a highly focused, lean organization centered on managing its partnership with Pierre Fabre Laboratories and advancing its remaining clinical pipeline.

Here's the quick math on the shift: Atara anticipates its full-year 2025 operating expenses will decrease by at least 60% compared to 2024, driven by this transition and subsequent cost-cutting measures.

  • Partnership-Centric Model: Substantially all tab-cel activities, including manufacturing, development, and BLA sponsorship, were transitioned to Pierre Fabre Laboratories in 2025. This move eliminates significant recurring operational costs for Atara.
  • Value Realization: The company's immediate financial focus is on the potential $40 million milestone payment contingent upon FDA approval of the tab-cel BLA. This payment, combined with the cash, cash equivalents, and short-term investments of $13.7 million as of September 30, 2025, is projected to provide significant cash runway.
  • Lean Workforce: A strategic organizational restructuring in October 2025 impacted approximately 29% of the workforce, retaining only about 15 employees essential for executing remaining strategic priorities.
  • R&D Focus: Research and development expenses were drastically reduced to $2.9 million for the third quarter of 2025, down from $43.9 million in the same period in 2024, reflecting the winding down of the allogeneic CAR-T programs (like ATA3219) and the transfer of tab-cel costs.

If you're looking for a deeper dive into the numbers, you can read Breaking Down Atara Biotherapeutics, Inc. (ATRA) Financial Health: Key Insights for Investors.

Atara Biotherapeutics, Inc.'s Strategic Advantages

Atara's competitive edge is now almost entirely concentrated in its proprietary T-cell platform and the financial structure of its lead asset.

  • Allogeneic T-Cell Platform: The core technology delivers off-the-shelf T-cell immunotherapies, which are ready-to-use and don't require the patient's cells, making them faster, more scalable, and logistically simpler than autologous cell therapies.
  • Pioneering Regulatory Approval: Atara was the first company in the world to receive regulatory approval for an allogeneic T-cell immunotherapy (Ebvallo™ in the European Economic Area), defintely a key validation of the platform.
  • EBV-Specific Targeting: The platform is uniquely designed to target the Epstein-Barr virus, which is the root cause of certain cancers and is implicated in autoimmune diseases like Multiple Sclerosis, providing a highly differentiated therapeutic approach.
  • High-Value Commercial Partnership: The global partnership with Pierre Fabre Laboratories for tab-cel/Ebvallo™ provides a clear path to market and non-dilutive funding via milestone payments and double-digit tiered royalties on net sales, reducing Atara's financial and operational risk.

Atara Biotherapeutics, Inc. (ATRA) How It Makes Money

Atara Biotherapeutics, Inc. makes money primarily through strategic collaboration and licensing agreements for its allogeneic T-cell immunotherapies (off-the-shelf cell therapies). The near-term financial engine is driven by significant milestone payments from partners like Pierre Fabre Laboratories, which will eventually transition to tiered royalties on net sales once their lead product, tabelecleucel (tab-cel), achieves full regulatory approval and commercialization.

Atara Biotherapeutics' Revenue Breakdown

The company's revenue structure has undergone a dramatic, planned shift in 2025 following the transfer of its lead asset, tab-cel, to Pierre Fabre Laboratories. This change eliminated recurring partnership payments, causing a sharp year-over-year decline in reported revenue, but setting the stage for future, high-margin milestone and royalty income. The total reported revenue for the third quarter of 2025 (Q3 2025) was $3.5 million.

Revenue Stream % of Total (Q3 2025) Growth Trend (Current vs. Prior Year)
Commercialization Revenue (Partnership/Deferred) 100% Decreasing (Down 91.4% YoY)
Milestone Payments & Royalties (Contingent) 0% (Near-term potential) Increasing (Future high-value events)

Here's the quick math: Q3 2025 commercialization revenue of $3.5 million was a 91.4% decrease from the $40.2 million reported in Q3 2024. This decline is not a commercial failure; it's the accounting result of recognizing upfront and deferred revenue in 2024 and Q1/Q2 2025 as manufacturing and regulatory responsibilities for tab-cel were transferred to Pierre Fabre Laboratories.

Business Economics

The core economic model has pivoted from a high-burn, integrated research and development (R&D) and manufacturing operation to an ultra-lean, royalty-based structure. This is a common, smart move for a biotech firm with a validated asset but limited cash. The company is now essentially a streamlined R&D shop focused on its next-generation platform, while its partner handles the costly commercialization. Mission Statement, Vision, & Core Values of Atara Biotherapeutics, Inc. (ATRA).

  • Pricing Strategy: Cell therapies like tab-cel (known as Ebvallo™ in Europe) command premium pricing due to their highly specialized nature and the lack of approved alternatives for conditions like Epstein-Barr virus positive post-transplant lymphoproliferative disease (EBV+ PTLD).
  • Cost Structure Shift: The strategic transfer of tab-cel activities to Pierre Fabre Laboratories has dramatically reduced operating expenses. R&D expenses, typically the largest cost for a biotech, plummeted 93% to just $2.9 million in Q3 2025, down from $43.9 million in the year-ago period. That's a massive, defintely necessary, cost-cutting measure.
  • Future Payouts: The most critical near-term economic event is the potential $40 million milestone payment from Pierre Fabre Laboratories, contingent upon the FDA approval of the tab-cel Biologics License Application (BLA), which has a target action date of January 10, 2026. This milestone is vital for the company's cash runway.

Atara Biotherapeutics' Financial Performance

The Q3 2025 financial results reflect a company in a deep strategic transition, prioritizing cash preservation and pipeline focus. The key takeaway is the dramatic reduction in the net loss, driven by the operational restructuring.

  • Net Loss Improvement: The net loss for Q3 2025 narrowed significantly to $4.3 million, an 80.4% improvement compared to the $21.9 million net loss in Q3 2024. This is a direct result of the workforce reduction (approximately 29% in October 2025) and the cost transfer.
  • Cash Position: As of September 30, 2025, cash, cash equivalents, and short-term investments totaled $13.7 million. This cash position is acutely tight, especially considering the net cash used in operating activities was $9.8 million for Q3 2025.
  • Operating Expense Guidance: Management projects that total operating expenses for the full fiscal year 2025 will be cut by at least 60% year-over-year, confirming the company's commitment to an ultra-lean operational model.

What this estimate hides is the binary nature of the $40 million milestone payment; without that capital, the financial picture changes rapidly. Finance: monitor the FDA's decision on the tab-cel BLA closely, as it dictates the company's cash runway past Q1 2026.

Atara Biotherapeutics, Inc. (ATRA) Market Position & Future Outlook

Atara Biotherapeutics, Inc. is at a critical inflection point in late 2025, shifting its focus from a high-burn R&D model to a royalty-and-milestone-driven structure centered on its lead allogeneic T-cell therapy (off-the-shelf) product, tabelecleucel (Ebvallo). The company's future trajectory hinges almost entirely on the pending US Food and Drug Administration (FDA) approval of its Biologics License Application (BLA) for tab-cel, which has a Prescription Drug User Fee Act (PDUFA) target action date of January 10, 2026. Getting this approval would immediately unlock a $40 million milestone payment from partner Pierre Fabre Laboratories, materially extending the cash runway beyond the $13.7 million reported in cash reserves as of September 30, 2025.

This strategic pivot, including a projected operating expense reduction of at least 60% for the full year 2025 compared to 2024, is a necessary reset. The market is watching closely, so the next few months are defintely make-or-break for shareholder value.

Competitive Landscape

In the nascent allogeneic T-cell therapy market, Atara holds a leading position based on a key regulatory win, but it faces competitors with more diverse pipelines and larger market capitalizations. While direct market share for a pre-commercial US product is tricky to calculate, estimates place Atara's share of the overall allogeneic T-cell therapies market at the higher end among pure-play companies. Here's the quick math on how the key players stack up in this niche, high-growth sector, which is projected to be valued at approximately $1.26 billion in 2025.

Company Market Share, % Key Advantage
Atara Biotherapeutics, Inc. 12-16% First regulatory approval for an allogeneic T-cell therapy (Ebvallo in EEA); non-CAR T-cell platform.
Allogene Therapeutics 10-14% Broadest allogeneic CAR T-cell pipeline (e.g., ALLO-501A, ALLO-329); higher market cap (~$265.18M).
Fate Therapeutics 6-10% Induced Pluripotent Stem Cell (iPSC) platform; strong focus on autoimmune diseases (FT819) with non-chemo conditioning.

Opportunities & Challenges

You need to map the near-term landscape to understand the stock's volatility. The biggest opportunity is a clear, near-term catalyst-the FDA decision-but the financial risk is just as clear without it. The company is actively exploring strategic alternatives, which could lead to a merger or acquisition, but that process is inherently uncertain.

Opportunities Risks
FDA approval of tab-cel (PDUFA Jan 10, 2026) in EBV+ PTLD, a high-unmet-need indication. Critical dependence on the $40 million BLA approval milestone for cash runway extension.
Immediate receipt of $40 million milestone payment plus double-digit tiered royalties from Pierre Fabre Laboratories. Low cash position of $13.7 million (Q3 2025) before the milestone, raising going-concern questions if approval is delayed.
Leveraging the off-the-shelf allogeneic platform for autoimmune diseases, a massive, emerging market. Intense competition from larger-cap, well-funded rivals like Allogene Therapeutics and Fate Therapeutics in the broader allogeneic space.

Industry Position

Atara Biotherapeutics, Inc. is positioned as a first-mover in the allogeneic T-cell immunotherapy space, specifically with a product that is already approved in Europe (Ebvallo) for a rare, life-threatening condition. This is a huge differentiator. The company's focus on Epstein-Barr virus (EBV) as a root cause for multiple diseases gives it a unique, targeted platform compared to the broader CAR T-cell approaches of its rivals.

  • Dominant in EBV-driven oncology: tab-cel targets EBV+ PTLD, a niche where no FDA-approved therapies exist.
  • Capital efficiency shift: Transitioning tab-cel costs to Pierre Fabre Laboratories is projected to cut 2025 operating expenses by over 60%, moving the company toward a leaner, royalty-based model.
  • Market capitalization: At $94.038 million (as of Nov 13, 2025), the company is a micro-cap, making it a potential acquisition target, especially for its first-in-class regulatory asset and platform technology.

To be fair, the company's recent workforce reductions, including a 29% cut in October 2025, show the extreme financial pressure it has been under. Still, the imminent BLA decision makes it a high-risk, high-reward proposition. For a deeper dive into the institutional ownership behind this unique biotech play, you should check out Exploring Atara Biotherapeutics, Inc. (ATRA) Investor Profile: Who's Buying and Why?

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